# Hyperbaric oxygen therapy attenuates urethral stricture formation after urethral injury: an experimental rabbit study

**Authors:** Hasan Danış, Alpaslan Yüksel, Dursun Baba, Yusuf Şenoğlu, Arda Taşkın Taşkıran, Ekrem Başaran, Ali Tekin, Sinem Kantarcıoğlu Coşkun

PMC · DOI: 10.1007/s00345-026-06323-2 · World Journal of Urology · 2026-03-04

## TL;DR

Hyperbaric oxygen therapy reduced urethral scarring and narrowing in rabbits after injury, suggesting it could help prevent this condition in humans.

## Contribution

This study is the first to demonstrate that hyperbaric oxygen therapy can reduce fibrosis and stricture formation in an experimental urethral injury model.

## Key findings

- Hyperbaric oxygen therapy significantly reduced urethral narrowing compared to untreated injury.
- Fibrosis scores were significantly lower in the hyperbaric oxygen group compared to the control group.
- Urethral diameters in the HBO group were closer to normal compared to the untreated injury group.

## Abstract

Urethral stricture (US) is a frequent and challenging urological entity characterized by spongiofibrosis and luminal narrowing, often leading to recurrent infections, urinary retention, and upper tract deterioration. Despite various endoscopic and open surgical options, high recurrence rates remain a major problem, and there is no established medical therapy to prevent stricture formation. To investigate the protective effect of hyperbaric oxygen (HBO) therapy on fibrosis and stricture formation in an experimental urethral injury model in rabbits using objective endoscopic, radiologic, and histopathologic parameters.

Twenty-eight male New Zealand rabbits were randomized into three groups: sham (n = 8), urethral injury without treatment (control, n = 10), and urethral injury plus HBO (HBO, n = 10). Among the 20 rabbits with urethral injury, allocation to the untreated control group (Group 2) and the HBO treatment group (Group 3) was performed in a 1:1 ratio using a computer-generated randomization list. Standardized circumferential electrocoagulation was applied to the bulbar urethra in the control and HBO groups. HBO was administered at 2 ATA, 90 min/day for 21 consecutive days starting on the day of injury. On day 28, all animals underwent urethroscopy and retrograde urethrography; urethral specimens were then harvested for histopathological evaluation. Fibrosis was graded (0–3) using Masson trichrome staining.

Normal urethral diameters were similar among the groups (p = 0.604). Median stricture diameter was significantly lower in the untreated control group compared with the HBO and sham groups (2.15 mm vs. 8.05 mm and normal segment, respectively; p < 0.001). Median percentage urethral narrowing was 78.52% in the control group and 23.51% in the HBO group (p < 0.001). Fibrosis scores were significantly higher in the control group than in the HBO and sham groups (p < 0.001).

HBO therapy significantly attenuated fibrosis and urethral narrowing in this experimental urethral injury model. These findings suggest that HBO may represent a promising adjuvant strategy to prevent US formation after urethral trauma, warranting further clinical investigation.

## Linked entities

- **Diseases:** urethral stricture (MONDO:0002127)
- **Species:** Oryctolagus cuniculus (taxon 9986)

## Full-text entities

- **Genes:** EPO [NCBI Gene 100008786], VEGFA (vascular endothelial growth factor A) [NCBI Gene 100008899] {aka VEGF, VEGFA165b}
- **Diseases:** Fibrosis (MESH:D005355), soft tissue infections (MESH:D018461), injury (MESH:D014947), periurethral abscess (MESH:D000038), inflammation (MESH:D007249), US (MESH:D014525), acute urinary retention (MESH:D016055), epididymitis (MESH:D004823), bladder stones (MESH:D001744), pain (MESH:D010146), fracture (MESH:D050723), chronic renal failure (MESH:D007676), CO poisoning (MESH:D011041), renal failure (MESH:D051437), impairment of (MESH:D060825), oedema (MESH:C536897), infection (MESH:D007239), dilation (MESH:D002311), Urethral injury (MESH:D014526), oesophageal injury (MESH:D000077277), ulceration (MESH:D014456), hydronephrosis (MESH:D006869), anorexia (MESH:D000855), dehydration (MESH:D003681), orchitis (MESH:D009920), lethargy (MESH:D053609), urinary tract infection (MESH:D014552), scrotal-perineal abscess (MESH:D009437), hypoxic (MESH:D002534), mucosal damage (MESH:D052016), interstitial cystitis (MESH:D018856), hypertrophic (MESH:D002312), bladder perforation (MESH:D001745), hypospadias (MESH:D007021), distress (MESH:D012128), Fournier's gangrene (MESH:D018934), fistula (MESH:D005402), ischaemia (MESH:D007511), stenosis (MESH:D003251), sepsis (MESH:D018805), radiation cystitis (MESH:D011832), prostatitis (MESH:D011472), overdose (MESH:D062787)
- **Chemicals:** triamcinolone (MESH:D014221), H&amp;E (MESH:D006371), Hematoxylin-eosin (-), paraffin (MESH:D010232), oxygen (MESH:D010100), mitomycin C (MESH:D016685), haematoxylin (MESH:D006416), xylazine (MESH:D014991), Carbon monoxide (MESH:D002248), dexpanthenol (MESH:C007288), halofuginone (MESH:C010176), ketamine (MESH:D007649), meloxicam (MESH:D000077239), eosin (MESH:D004801), tadalafil (MESH:D000068581), pO2 (MESH:C093415), NaOH (MESH:D012972), povidone-iodine (MESH:D011206), formaldehyde (MESH:D005557)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606], Oryctolagus cuniculus (domestic rabbit, species) [taxon 9986]

## Full text

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## Figures

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## References

3 references — full list in the complete paper: https://tomesphere.com/paper/PMC12960306/full.md

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Source: https://tomesphere.com/paper/PMC12960306